"68001-236-03" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-236-03)
(BluePoint Laboratories)

NDC Code68001-236-03
Package Description500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-236-03)
Product NDC68001-236
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140224
Marketing Category NameANDA
Application NumberANDA077715
ManufacturerBluePoint Laboratories
Substance NameBUPROPION HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesAminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-236-03